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barbara5452

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Everything posted by barbara5452

  1. What a great friend of Lenny and his wife. Direct them this way...
  2. Great answer Trish. I like those two NED's too.
  3. MM, I can already tell your hubby is a lucky man, you go girl....Keep in touch..
  4. GREAT ATTITUDE ! praying for good results...
  5. Vivian welcome, my mother was distance with her illness also, just support and do what she allows and let her share when she is ready. God Bless..
  6. Dusti, so sorry for your loss. Quilt or regrets are something you should not have. Sounds like you did all you we able to do. God Bless...
  7. Ditto with all the above, tell us alittle more about yourself and feel free to vent anytime. Welcome.
  8. Prayers will be sent, wow what a story, being my second round of cancer that is very promising for me. Thank you so much for sharing, now go win the fight again.
  9. Sorry you have to be here, your sister is lucky to have you. I was told if surgery is possible that is a good thing. I have a friend who is going on her 7th year and her tumor was the size of a grapefruit when found. And that was her second bout with cancer. She is doing wonderful. Tell her not to give up and to read some of the post on this site, it really will help her deal a bit better.
  10. For me and test times I seem to hum and sing in my mind, Doris Day "K sara sara what ever will be will be the futures not ours to see K sara sara" And when I get the report I wanted it's Margaritaville Jimmy Buffet.
  11. Welcome, you have already received some wonderful advise and opinions, when feeling discouraged come back and read them over and over that is what I do when I post negative and get such a tremendous uplifting comments from these wonderful people. Again welcome.
  12. Bobbi, Sorry you have to be here, I teared up reading your post because it brought back the memories of the lost I too felt and still do at times but as time goes on we learn to cope better. Don't give up and as said above once a plan is in place you will feel better and get your boxing gloves on. HUGS !!!
  13. Welcome aboard Jon, keep up updated with your onc. visits.
  14. Hi, sorry I have no insite on that drug, although I am sure someone here in the group will proberly know. What is the history with your husband ? And what stage is he ? This is a great lung cancer community and I am sure you will find many answers to your questions here. Again welcome.
  15. Welcome Connie, I too was like you, lets get this all started so we can be finished (chemo/rad) Best of luck.....
  16. Prayers for your close family and dad, let us know what the onc. thinks about the tea...
  17. Hi Trudy, welcome to our world, it will get easier, I too take zoloft have been on it for over 10 years for depression and PMDD, it does help but I did find I needed additional help with my recurrence so my pcp prescribed Klonpin which has help alot, without out it I found myself at a pity party nearly everyday. You will find each week is a bit better, I too am stage IIIB with the recurrence. Went for a CT scan this morning now doing the Www Waiting wondering watching game. We are here whenever you need us, there is always someone on this site night and day. I have trouble sleeping at times and find myself looking for posts up in the late hours. Prayers that you find some peace soon.,,,
  18. Anger one of the many emotions you will encounter, My today's anger bring some sense of acceptance tomorrow. Welcome, and vent anytime. PRAYERS your way.
  19. Ned, as I finish reading your wonderful post this a.m you shared your peace with me. Thank you. It is going to be a wonderful day. Thank you again...
  20. Big welcome Mike and tell you wife you will be the computer whiz and she can dictate. Glad you found us.
  21. Welcome, your mom is a lucky lady to have such a wonderful daughter looking after her. Even though school has started it sounds like you have gotten her thru her big hurdle and if she needs you by her side again you will know. Keep us updated
  22. Sorry for the news you received on grand dad, Don't give up just yet. How old are you ? You are welcome to talk to us anytime. Welcome aboard.
  23. Lung cancer is never at the topped because it's etched in peoples minds that it is a self induced cancer and as we all know in this site that is SO UNTRUE, I hope in my lifetime to see that changed it is very discouraging for us that have or know someone with the desease.
  24. Katie, thanks so much for all you do, we all think it but sometimes forget to say it. So here it is. We love you !
  25. I too would leave it to your parents they will know when you are most needed, FLMA can only be taken for 6 months so timing has to be as just right. But you must always trust your heart and set your own priorities also on what you feel is right. I agree the conversation needs to take place for a decision to be made. When my mother took ill and my sister and I took turns caring for her, taking FLMA was a decision I never regreted. Take care.
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